Supply of Doxycyline by Community Pharmacists to Patients with an Exacerbation of COPD Protocol Number 476 Version 1

Transcription

1 Supply of Doxycyline by Community Pharmacists to Patients with an Exacerbation of COPD Protocol Number 476 Version 1 Date protocol prepared: March 2016 Date protocol due for review: March 2018 This patient group direction must be signed by all health care professionals involved in its use. NHS Forth Valley should hold the original signed copy. The PGD must be easily accessible in the clinical setting. Organisation NHS Forth Valley Job Title Name Signature Date Director of Nursing Angela Wallace Signed by Angela Wallace 9/5/16 Medical Director Tracey Gillies Signed by Tracey Gillies 9/5/16 Director of Pharmacy Gail Caldwell Signed by Gail Caldwell 10/5/16 This document authorises the supply of doxycycline by appropriate practitioners to patients who meet the criteria for inclusion under the terms of the document. Practitioners seeking to supply doxycycline must ensure that they assess all clients to make sure they meet the criteria before supplying the product. The purpose of this Patient Group Direction is to help patients by ensuring that they have ready access to a quality assured service which provides a timely, consistent and appropriate supply of doxycycline for an infective exacerbation of COPD.

2 Signatures of those developing the Patient Group Direction Job Title Name Signature Date Doctor Dr. William Newman Signed by William Newman 20/4/16 Pharmacist Clare Colligan Signed by Clare Colligan 15/4/16 Nurse Microbiologist (if appropriate) Paediatrician (if appropriate) Dr. Sara. Jamdar Signed by Sara Jamdar 6/5/16 NA Approval from Patient Group Directions Group Chair Signed on behalf of group Date Patient Group Directions Group Gail Caldwell Signed by Gail Caldwell 10/5/16 2 -

3 The following Patient Group Direction for Supply of Doxycycline by Community Pharmacists to patients with an exacerbation of COPD may be used from the following business/practice: Name: Address: YOU MUST BE AUTHORISED BY NAME, UNDER THE CURRENT VERSION OF THIS PGD BEFORE YOU ATTEMPT TO WORK ACCORDING TO IT CLINICAL CONDITION Indication To allow Community Pharmacists to supply doxycycline to patients with an infective exacerbation of Chronic Obstructive Pulmonary Disease (COPD) who have an allergy to penicillin. Inclusion Criteria Definite diagnosis of COPD Infective exacerbation characterised by development or increase in sputum purulence and one or more of the following - increase in shortness of breath - increase in sputum volume Patient has Forth Valley COPD self-management plan agreed with GP which allows for treatment from Community Pharmacist Exclusion Criteria 1. Known allergy to doxycycline 2. Pregnancy 3. Breast Feeding 4. Patients with rare hereditary problems of fructose intolerance, glucose galactose malabsorption or sucroseisomaltase insufficiency. 5. Myasthenia gravis 6. Systemic lupus erythematosus (SLE) 7. Patients receiving the following medications; methotrexate, oral ciclosporin, oral retinoids. 8. Patients taking ergotamine or methysergide 9. Course of antibiotics within the last month with no resolution of symptoms 10. More than 2 supplies by community pharmacist in any 3 month period 11. Patient does not have Forth Valley COPD selfmanagement plan at time of presentation Caution/ Need for 1. The absorption of doxycycline may be impaired by further advice concurrently administered antacids containing aluminium, calcium, magnesium or other drugs containing these cations; oral zinc, iron salts or bismuth preparations. Dosages should be maximally separated. 2. For patients taking warfarin - advise patient to contact GP Practice as soon as practical to arrange to have INR checked. Action if Patient declines or is excluded Refer patient to GP or Out of Hours via Professional to Professional Line 3 -

4 DRUG DETAILS Name, form & strength of medicine Legal Status Route/ Method Dosage Frequency Duration of treatment Maximum or minimum treatment period Quantity to Supply/ administer Side Effects Doxycycline 100mg capsules POM Oral 200mg day 1 then 100mg daily Daily 5 days 6 The following adverse reactions have been observed in patients receiving tetracyclines, including doxycycline. Infections and infestations Superinfection: As with all antibiotics, overgrowth of nonsusceptible organisms may cause candidiasis, glossitis, staphylococcal enterocolitis, pseudomembranous colitis (with Clostridium difficile overgrowth) and inflammatory lesions (with candidal overgrowth) in the anogenital region. Blood and lymphatic system disorders Haemolytic anaemia, thrombocytopenia, neutropenia, porphyria, and eosinophilia have been reported with tetracyclines. Immune system disorders Hypersensitivity reactions, including anaphylactic shock, anaphylaxis, anaphylactoid reaction, anaphylactoid purpura, hypotension, pericarditis, angioneurotic oedema, exacerbation of systemic lupus erythematosus, dyspnoea, serum sickness, peripheral oedema, tachycardia and urticaria. Endocrine disorders When given over prolonged periods, tetracyclines have been reported to produce brown-black microscopic discolouration of thyroid tissue. No abnormalities of thyroid function are known to occur. Nervous system disorders Headache, bulging fontanelles in infants and benign intracranial hypertension in juveniles and adults have been reported in individuals receiving full therapeutic dosages of tetracyclines. In relation to benign intracranial hypertension, symptoms included blurring of vision, scotomata diplopia and permanent visual loss has been reported. Ear and labyrinth disorders Tinnitus Gastrointestinal disorders Gastrointestinal symptoms are usually mild and seldom necessitate discontinuation of treatment. They include: abdominal pain, stomatitis, anorexia, nausea, vomiting, diarrhoea, dyspepsia and rarely dysphagia. Oesophagitis and oesophageal ulceration have 4 -

5 been reported in patients receiving doxycycline. A significant proportion of these occurred with the hydrochloride salt in the capsule form. Tetracyclines may cause discoloration of teeth and enamel hypoplasia, but usually only after long-term use. Hepatobiliary disorders There have been rare reports of hepatotoxicity with transient increases in liver function tests, hepatitis, jaundice, hepatic failure and pancreatitis. Skin and subcutaneous tissue disorders Rashes including maculopapular and erythematous rashes, exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome and toxic epidermal necrolysis have been reported. Photosensitivity skin reactions and photo-onycholysis. Musculoskeletal and connective tissue disorders Arthralgia and myalgia Renal and urinary system disorders Increased blood urea Reproductive system and breast disorders Vaginitis For a full list of side effects refer to Summary of Product Characteristics. A copy of this must be available to the health professional administering medication under this Patient Group Direction This can be accessed at Patients experiencing any adverse effects should discuss this with their GP or Community Pharmacist. All adverse reactions that are serious or result in harm should be reported to the MHRA through the Yellow Card Scheme. Advice to patient/carer Follow up Inform patients of possible side effects and their management. The Drug Manufacturer Patient Information Leaflet should be given. Patients taking antacids containing aluminium, calcium, magnesium or other drugs containing these cations; oral zinc, iron salts or bismuth preparations should be advised to avoid taking these at the same time as doxycyline. Patients receiving warfarin should be advised to have their INR checked. Patients not improving after a few days of starting antibiotic course or if any deterioration should be advised to contact GP or OOH service. STAFF CHARACTERISTICS Qualifications Pharmacist whose name is currently on the practising section of the pharmaceutical register held by The General Pharmaceutical Council 5 -

6 Specialist competencies or Qualifications Attendance at local training events on COPD. Completion of NES COPD interactive resource via NES Portal Continuing Training & Education Up to date knowledge in therapeutic area REFERRAL ARRANGEMENTS & AUDIT TRAIL Referral arrangements Patients who are not improving or feel their condition is getting worse should seek urgent treatment from their GP or through NHS24 out of hours Records/audit trail Record of supply must be made on PMR and in the patient s selfmanagement card. This should include the date of supply, the dosing instructions and the advice given re side effects and follow up. The record on the PMR should include the name of the pharmacist making the supply and criteria satisfied for supply i.e. presenting symptoms A computer or manual record of all patients receiving doxycycline through this PGD must be kept for audit purposes. Reference sources and comments The patient s GP must be made aware of the supply within 72 hours of supply being made using the agreed pro-forma. 1. Chronic Obstructive Pulmonary Disease. National clinical guideline on management of chronic obstructive pulmonary disease in adults in primary and secondary care. CG101. June Global Initiative for Chronic Obstructive Lung Disease. Global Strategy for Diagnosis, Management and Prevention of COPD ( 3. BNF Current Edition 4. Summary of product characteristics 6 -

7 PATIENT GROUP DIRECTION AUTHORISATION DOCUMENT Supply of Doxycycline capsules by Community Pharmacists to Patients with an Exacerbation of COPD Protocol Number 476 version 1 Individual Authorisation This PGD does not remove inherent professional obligations or accountability It is the responsibility of each professional to practice only within the bounds of their own competence and in accordance with their own Code of Professional Conduct. It is also your responsibility to ensure that all consultations with patients occur within a private and confidential area of the pharmacy. I have read and fully understand the Patient Group Direction for the supply of Doxycycline capsules and agree to provide this medicine only in accordance with this PGD in NHS Forth Valley Community Pharmacies. Name of Pharmacist GPhC Number Normal Pharmacy Location (including contractor code) Signature Date The above person has been authorised to use this protocol Signature of Authorising Pharmacist on behalf of Employing Organisation Name Signature Date Note : A copy of this agreement must be signed by each pharmacist who wishes to be authorised to use the PGD for Supply of Doxycycline capsules by Community Pharmacists working in Forth Valley Pharmacies. Please return this form (page 8) to Pharmacy Services, Falkirk Community Hospital, Westburn Avenue, Falkirk. FK1 5QE Fax and retain a copy in each pharmacy premises they wish to provide the medicine from. A copy of the PGD must also be available in the pharmacy for reference. Each authorised pharmacy practitioner should be provided with an individual copy of the clinical content of the PGD and a photocopy of the document showing their authorisation. 7 -